School of Pharmacy, Provincial and State Key Laboratory Breeding Base of System Research, Development and Utilization of Chinese Herbal Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Department of Pharmacy, 302 Hospital of People's Liberation Army, Beijing, China.
J Pharm Pharmacol. 2018 Dec;70(12):1675-1687. doi: 10.1111/jphp.13008. Epub 2018 Sep 14.
OBJECTIVES: Cholestasis is a critical risk factor for severe hepatic disease or cirrhosis. The anti-inflammatory effect of Paeonia lactiflora Pall. (PLP), named Chishao in traditional Chinese medicine (TCM), on alpha-naphthylisothiocyanate (ANIT)-induced cholestasis model was tried to be elucidated in this research. METHODS: Therapeutic effect indices on hepatic function, including ALT, AST, TBIL, DBIL, ALP, TBA and γ-GT, were measured. To further investigate the protective mechanism of PLP, the mRNA and protein expression levels of NF-κB-NLRP3 inflammasome pathway were detected. RESULTS: Our results showed that compared with the model group, PLP could significantly reduce the increased serum indices such as ALT, AST, TBIL, DBIL, ALP, TBA and γ-GT induced by ANIT in a dose-dependent way. Moreover, we found that PLP downregulated the mRNA expression levels including IKK, p65, NLRP3, caspase-1 and IL-1β, especially at the large dose. Furthermore, PLP also significantly inhibited NF-κB-NLRP3 inflammasome pathway by decreasing the protein levels of p65, p-p65, p-IKK, NLRP3, caspase-1 and IL-1β. CONCLUSIONS: The results indicated that PLP could ameliorate ANIT-induced cholestasis in rats and the anti-inflammatory effect of PLP might be related to regulating NF-κB-NLRP3 inflammasome pathway. This study will provide scientific evidence for PLP as a potential drug candidate for cholestasis.
目的:胆汁淤积是导致严重肝疾病或肝硬化的关键危险因素。本研究旨在探讨白芍(白芍在中医中称为赤芍)对α-萘异硫氰酸酯(ANIT)诱导的胆汁淤积模型的抗炎作用。
方法:测定肝功能的治疗效果指标,包括 ALT、AST、TBIL、DBIL、ALP、TBA 和 γ-GT。为进一步探讨 PLP 的保护机制,检测 NF-κB-NLRP3 炎性小体通路的 mRNA 和蛋白表达水平。
结果:与模型组相比,PLP 能显著降低 ANIT 诱导的大鼠血清 ALT、AST、TBIL、DBIL、ALP、TBA 和 γ-GT 等指标的升高,且呈剂量依赖性。此外,我们发现 PLP 能下调 IKK、p65、NLRP3、caspase-1 和 IL-1β 的 mRNA 表达水平,尤其是大剂量时。此外,PLP 还通过降低 p65、p-p65、p-IKK、NLRP3、caspase-1 和 IL-1β 的蛋白水平,显著抑制 NF-κB-NLRP3 炎性小体通路。
结论:结果表明,PLP 能改善 ANIT 诱导的大鼠胆汁淤积,PLP 的抗炎作用可能与调节 NF-κB-NLRP3 炎性小体通路有关。本研究为 PLP 作为胆汁淤积潜在药物候选物提供了科学依据。
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